2C-I
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2C-I
Summary
2C-I is a type of chemical entity[1]. 2C-I ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (123 views/month).[2]
Key Facts
- 2C-I is credited with the discovery of Alexander Shulgin[3].
- 2C-I's image is recorded as 2C-I Powder.jpg[4].
- 2C-I's instance of is recorded as type of chemical entity[5].
- 2C-I's main regulatory text is recorded as Betäubungsmittelgesetz[6].
- 2C-I's chemical structure is recorded as 2,5-Dimethoxy-4-iodphenethylamin.svg[7].
- 2C-I's chemical structure is recorded as 2C-I.svg[8].
- 2C-I's CAS Registry Number is recorded as 69587-11-7[9].
- 2C-I's EC number is recorded as 690-397-2[10].
- 2C-I's canonical SMILES is recorded as COC1=CC(=C(C=C1CCN)OC)I[11].
- 2C-I's InChI is recorded as InChI=1S/C10H14INO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3[12].
- 2C-I's InChIKey is recorded as PQHQBRJAAZQXHL-UHFFFAOYSA-N[13].
- 2C-I's chemical formula is recorded as C₁₀H₁₄INO₂[14].
- 2C-I's subclass of is recorded as 2C[15].
- 2C-I's Commons category is recorded as 2C-I[16].
- 2C-I's has part is recorded as nitrogen[17].
- 2C-I's has part is recorded as carbon[18].
- 2C-I's has part is recorded as hydrogen[19].
- 2C-I's has part is recorded as iodine[20].
- 2C-I's has part is recorded as oxygen[21].
- 2C-I's has part is recorded as phenyl group[22].
- 2C-I's ChEMBL ID is recorded as CHEMBL338297[23].
- 2C-I's Freebase ID is recorded as /m/021m1g[24].
- 2C-I's UNII is recorded as S35362848V[25].
- 2C-I's ChemSpider ID is recorded as 8442670[26].
- 2C-I's PubChem CID is recorded as 10267191[27].
Body
Works and Contributions
2C-I is credited with the discovery of Alexander Shulgin[3].
Why It Matters
2C-I ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (123 views/month).[2] 2C-I has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] 2C-I is known by 9 alternative names across languages and contexts.[29]